N-Heterocyclic Carbene Analogues of Wittig Hydrocarbon.

N-Heterocyclic carbene (NHC) analogues of Wittig hydrocarbon, [(NHC)(Stil)(NHC)] (3a-c) (NHC = SIPr (1a) = C[N(Dipp)CH2]2, Dipp = 2,6-iPr2C6H3; IPr (1b) = C[N(Dipp)CH]2; Me-IPr (1c) = C[N(Dipp)CMe]2 and Stil = C6H4CHCHC6H4) have been reported as crystalline solids. 3a-c are prepared by two-electron reductions of the corresponding bis-1,3-imidazoli(ni)um bromides [(NHC)(Stil)NHC)](Br)2 (2a-c) with KC8 in >94 % yields. 2a-c are accessible by the nickel catalyzed direct C-C coupling of NHCs (1a-c) with (E)-4,4'-dibromostilbene. One-electron oxidation of 3a,b yields the corresponding radical cations [(NHC)(Stil)NHC)]B(C6F5)4 4a,b. All compounds have been characterized by UV-Vis/NMR/EPR spectroscopy as well as 2a, 3a, and 3b by single crystal X-ray diffraction. The electronic structures of representative systems have been analyzed by quantum chemical calculations.

Isolation of an Annulated 1,4-Distibabenzene Diradicaloid.

The first 1,4-distibabenzene-1,4-diide compound [(ADC)Sb]2 (5) based on an anionic dicarbene (ADC) (ADC=PhC{N(Dipp)C}2 , Dipp=2,6-iPr2 C6 H3 ) is reported as a bordeaux-red solid. Compound 5, featuring a central six-membered C4 Sb2 ring with formally SbI atoms may be regarded as a base-stabilized cyclic bis-stibinidene in which each of the Sb atoms bears two lone-pairs of electrons. 5 undergoes 2 e-oxidation with Ph3 C[B(C6 F5 )4 ] to afford [(ADC)Sb]2 [B(C6 F5 )4 ]2 (6) as a brick-red solid. Each of the Sb atoms of 6 has an unpaired electron and a lone-pair. The broken-symmetry open-shell singlet diradical solution for (6)2+ is calculated to be 2.13 kcal mol-1 more stable than the closed-shell singlet. The diradical character of (6)2+ according to SS-CASSCF (state-specific complete active space self-consistent field) and UHF (unrestricted Hartree-Fock) methods amounts to 36 % and 39 %, respectively. Treatments of 6 with (PhE)2 yield [(ADC)Sb(EPh)]2 [B(C6 F5 )4 ]2 (7-E) (E=S or Se). Reaction of 5 with (cod)Mo(CO)4 affords [(ADC)Sb]2 Mo(CO)4 (8).

Isolation of an Arsenic Diradicaloid with a Cyclic C2 As2 -Core.

Herein, we report on the synthesis, characterization, and reactivity studies of the first cyclic C2 As2 -diradicaloid {(IPr)CAs}2 (6) (IPr = C{N(Dipp)CH}2 ; Dipp = 2,6-iPr2 C6 H3 ). Treatment of (IPr)CH2 (1) with AsCl3 affords the Lewis adduct {(IPr)CH2 }AsCl3 (2). Compound 2 undergoes stepwise dehydrochlorination to yield {(IPr)CH}AsCl2 (3) and {(IPr)CAsCl}2 (5 a) or [{(IPr)CAs}2 Cl]OTf (5 b). Reduction of 5 a (or 5 b) with magnesium turnings gives 6 as a red crystalline solid in 90% yield. Compound 6 featuring a planar C2 As2 ring is diamagnetic and exhibits well resolved NMR signals. DFT calculations reveal a singlet ground state for 6 with a small singlet-triplet energy gap of 8.7 kcal mol-1 . The diradical character of 6 amounts to 20% (CASSCF, complete active space self consistent field) and 28% (DFT). Treatments of 6 with (PhSe)2 and Fe2 (CO)9 give rise to {(IPr)CAs(SePh)}2 (7) and {(IPr)CAs}2 Fe(CO)4 (8), respectively.